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Targeted α Therapies for the Treatment of Bone Metastases

The skeleton is the target tissue for many types of tumors, and, recently, the survival of patients with prostate cancer metastasis has been increased using α-emitting drugs known as targeted α therapies. The use of α-radiopharmaceuticals in medicine was hypothesized at the beginning of the nineteen...

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Detalles Bibliográficos
Autores principales: Zustovich, Fable, Barsanti, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796024/
https://www.ncbi.nlm.nih.gov/pubmed/29283383
http://dx.doi.org/10.3390/ijms19010074
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author Zustovich, Fable
Barsanti, Roberto
author_facet Zustovich, Fable
Barsanti, Roberto
author_sort Zustovich, Fable
collection PubMed
description The skeleton is the target tissue for many types of tumors, and, recently, the survival of patients with prostate cancer metastasis has been increased using α-emitting drugs known as targeted α therapies. The use of α-radiopharmaceuticals in medicine was hypothesized at the beginning of the nineteenth century after the observation that α-radionuclides were associated with high cell-killing energy and low tissue penetration in healthy tissues. In the prostate cancer (PC) scenario, current research suggests that this class of radiopharmaceuticals has limited toxicity, and that the mechanism of action does not overlap with pre-existing drugs, allowing us to extend therapeutic armaments and address medical oncology towards personalized and precision medicine. Ongoing studies may extend these benefits also to bone metastases deriving from other neoplasms. The aim of this review is to summarize the current research on targeted α therapies and try to identify the right patient to be treated in the right time in order to integrate in these medications in the every-day clinical practice.
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spelling pubmed-57960242018-02-09 Targeted α Therapies for the Treatment of Bone Metastases Zustovich, Fable Barsanti, Roberto Int J Mol Sci Review The skeleton is the target tissue for many types of tumors, and, recently, the survival of patients with prostate cancer metastasis has been increased using α-emitting drugs known as targeted α therapies. The use of α-radiopharmaceuticals in medicine was hypothesized at the beginning of the nineteenth century after the observation that α-radionuclides were associated with high cell-killing energy and low tissue penetration in healthy tissues. In the prostate cancer (PC) scenario, current research suggests that this class of radiopharmaceuticals has limited toxicity, and that the mechanism of action does not overlap with pre-existing drugs, allowing us to extend therapeutic armaments and address medical oncology towards personalized and precision medicine. Ongoing studies may extend these benefits also to bone metastases deriving from other neoplasms. The aim of this review is to summarize the current research on targeted α therapies and try to identify the right patient to be treated in the right time in order to integrate in these medications in the every-day clinical practice. MDPI 2017-12-28 /pmc/articles/PMC5796024/ /pubmed/29283383 http://dx.doi.org/10.3390/ijms19010074 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zustovich, Fable
Barsanti, Roberto
Targeted α Therapies for the Treatment of Bone Metastases
title Targeted α Therapies for the Treatment of Bone Metastases
title_full Targeted α Therapies for the Treatment of Bone Metastases
title_fullStr Targeted α Therapies for the Treatment of Bone Metastases
title_full_unstemmed Targeted α Therapies for the Treatment of Bone Metastases
title_short Targeted α Therapies for the Treatment of Bone Metastases
title_sort targeted α therapies for the treatment of bone metastases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796024/
https://www.ncbi.nlm.nih.gov/pubmed/29283383
http://dx.doi.org/10.3390/ijms19010074
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